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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252240생성일: 2026년 10월 25일

Pyridine → 4-bromo-N-[(5-bromo-1,3-thiazol-2-yl)carbamoyl]-5-chlorothiophene-2-sulfonamide

https://huagongshe.com/reaction/252240

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Sodium CyanateHCID 517096—
반응물5-Bromothiazol-2-amine monohydrobromideHCID 2723848—
반응물4-Bromo-5-chlorothiophene-2-sulfonyl chlorideHCID 2797220—
촉매Acetic AcidHCID 176—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물4-bromo-N-[(5-bromo-1,3-thiazol-2-yl)carbamoyl]-5-chlorothiophene-2-sulfonamideHCID 24752361—

반응 단계

4-Bromo-5-chloro-thiophene-2-sulfonyl chloride (0.44 g, 1.50 mmol) and pyridine (0.27 ml, 3.40 mmol) were added to a stirred suspension of sodium cyanate (0.14 g, 2.20 mmol) in dry acetonitrile (1 ml) and the mixture stirred at room temperature for 4 hours. 5-Bromo-thiazol-2-ylamine hydrobromide (0.26 g, 1.00 mmol) was added and the reaction stirred for 30 minutes. Water (2 ml) and acetic acid (3 drops) were added. The resulting precipitate was filtered and the solid washed with water, cold methanol and diethyl ether. The solid was dried under reduced pressure to give 4-bromo-N-[(5-bromo-1,3-thiazol-2-yl)carbamoyl]-5-chlorothiophene-2-sulfonamide, 0.29 g (60%), m/e 477.8 (MH−).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868030B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-b7e58246bbc2468bb2c288d11cb2e1de
출처 메모uspto-grants-2011_01